5779-46-4

Upstream product

• 572-09-8 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide 
• 100-02-7 4-nitro-phenol 
• 30902-95-5 4-nitrophenyl 2,3,4,6-tetra-O-acetyl-D-glucopyranoside 
• 1262015-20-2 p-nitrophenyl 2,3,4,6-tetra-O-benzoyl-β-D-gulopyranoside 

Downstream Products

• 96192-22-2 (4-aminophenyl)-D-glucopyranoside 
• 16790-33-3 p-nitrophenyl 2-O-β-D-mannopyranosyl-β-D-mannopyranoside 
• 72647-96-2 p-nitrophenyl 6-O-β-D-mannopyranosyl-β-D-mannopyranoside 
• 1262015-21-3 p-nitrophenyl 4,6-O-benzylidene-β-D-gulopyranoside 

Relevant academic research and scientific papers

Syntheses and NMR and XRD studies of carbohydrate-ferrocene conjugates

Carbohydrate-ferrocene conjugates were synthesized and showed that the ferrocene entity appeared to be confined to a low volume so that proton NMR spectroscopy revealed 3 to 4 signals for substituted cyclopentadienyl instead of two usually.

Syntheses of p-nitrophenyl 3- and 4-thio-β-d-glycopyranosides

Thioglycosides have proved to be useful, enzymatically stable analogs of glycosides for structural and mechanistic studies and their synthesis is considerably simplified through the use of thioglycoligases. As part of an investigation into the use of thio